Doped Oxide Research Articles

Enhancing tetrafullerene based photosensors and photovoltaic cells by graphene oxide doping

This study explores the postulated potential of tetrafullerene as a charge transport material when combined with dispersed graphene oxide (GO), over concerns about fullerene’s limited performance in similar devices. Incorporating GO is expected to augment carrier concentration, increase surface area, and reduce operating voltages. Devices fabricated with p-Si/tetrafullerene with varying GO concentration exhibit notable enhancements in both dark and illuminated characteristics. The results demonstrate improved electron concentration and transport, leading to enhanced rectification ratios, ideality factors, and interface state densities across a broad bias and illumination range. Notably, devices doped with 0.2GO exhibit the most promising electrical and photoresponse characteristics, showcasing potential for applications in photosensing and photovoltaics.

Speckle Pattern Analysis of PVK:rGO Composite Based Memristor Device

AbstractThe memristors are expected to be fundamental devices for neuromorphic systems and switching applications. The device made of a sandwiched layer of poly(N‐ vinylcarbazole) and reduced graphene composite between asymmetric electrodes (ITO/PVK:rGO/Al) exhibits bistable resistive switching behavior. The performance of the memristor can be optimized by controlling the doped graphene oxide. To assess the device performance when it switches between ON and OFF states, optical characterization approaches are highly promising due to their non‐destructive and remote nature. Here, speckle pattern (SP) analysis to this end is introduced. SPs include a huge amount of information about their generating mechanism, which is extracted through statistical elaboration. SPs of the PVK:rGO in different states in situ and examine the conduction mechanism is acquired. The variations in the statistical parameters are attributed to the resistance state of the PVK:rGO with regard to the physical switching mechanism. The resistance/conduction state, in turn, depends on the activity and properties of PVK:rGO memristors, as well as the additional non‐uniformities induced through the variations of density of carriers. The present optical methodology can be potentially served as a bench‐top device for characterization purposes of similar devices during their operating.

Perovskite manganese oxide-based superposed multilayer film with high emittance tunability for smart radiation devices

Smart radiation devices (SRDs) with the ability to switch emittance according to the radiator surface’s temperature are significant for spacecraft thermal control on exploration missions with drastic changes in thermal environments. However, it is quite urgent to improve the performance of the intelligent thermal control films in SRDs due to the limitations such as low emittance tunability and inappropriate phase transition temperature. Consequently, a film with self-adaptive infrared emittance based on anti-reflective design is proposed in this paper. The main structure is a superposed multilayer film based on a doped perovskite manganese oxide La0.825Sr0.175MnO3 (LSMO) and BaF2 stacks. The emittances of the designed multilayer film are 0.18 and 0.83 at the temperatures of 100 K and 295 K, and therefore the emittance tunability achieves 0.65. Compared with single-layer LSMO, the emittance tunability has increased 25 % approximately. The enhancement in emittance tunability can be explained by the fact that multilayer films with staggered low and high refractive index dielectric layers may cause destructive interference and suppress the Fresnel reflections at high temperatures. In addition, the thickness of dielectric part is carefully designed to avoid the formation of high emissivity Fabry-Perot (FP) resonance when LSMO switches to metallic state at low temperatures. This perovskite manganese oxide-based multilayer film exhibits remarkable intelligent thermal control properties. It provides a significant opportunity to improve the performance of SRDs and a promising potential for maintaining the optimal operating temperature of the spacecraft.

(Invited) Solving the Energy Storage and Energy Conversion Conundrum – Materials to the Rescue

Energy storage systems have witnessed a meteoric rise ever since Sony commercialized the first Li-ion battery in 1994. Over the years, there have been a plethora of cathode, anode and electrolyte systems developed with stable cycle life and high coulombic efficiencies currently deployed in commercial electric vehicles. Similarly, alternate silicon and tin anodes were targeted as the next generation anodes to ubiquitous carbon. Recalcitrant volume expansion and ensuing solid electrolyte interphase (SEI) issues have reverted the focus back to the omnipresent high-energy density Li metal with efforts to overcome the ominous flammability and safety issues. Escalated impending demand for higher energy density have also made sulfur, an economic and common industrial effluent an attractive active material reverting attention back to Li-S batteries. Similarly, the portentous signs of global warming and the concomitant desire for developing green energy solutions have made hydrogen an imperative and attractive energy source providing the impetus for economic proton exchange membrane (PEM)-based water electrolysis (PEMWE) and fuel cells (PEMFCs). Like the energy storage field, PEMWE and PEMFCs have also witnessed intense research activity over the years following the early work on direct methanol fuel cells (DMFC). Developing high performance materials systems for energy storage and super responsive low-cost electrocatalysts still remain the major conundrum for developing high energy density and high-power density energy storage and conversion systems, respectively.This presentation will discuss the materials challenges that need to be overcome in Li-S batteries and PEM-based water electrolysis and fuel cells. Specifically, efforts aimed at achieving high-energy density cathodes and anodes as well as electrolyte additives for meeting the 500 Whkg-1 energy density targets for electric vehicle technology will be discussed. High sulfur (4-6 mg/cm2) loaded confined cathodes with unique ability to trap the pernicious polysulfide species combined with unique theoretical first principles calculations derived functional electrocatalysts exhibiting the propensity to reversibly catalyze the formation of Li2S and elemental S will be discussed. In tandem, progress made in generating new dendrite-free anodes and low-density current collectors exhibiting areal capacities as high as 15 mAh/cm2 with stable cycling over 100 cycles as well as electrolyte additives matching the cathode and anode performances will be outlined. Similarly, the journey into developing innovative low temperature chemical complexation approaches to novel bifunctional metallic nanostructured electrocatalysts first for DMFC systems and later how the unique approaches were modified targeting acid mediated PEMWE and PEMFCs comprising nanoscale metallic and complex ceramic doped oxide systems will be presented and discussed. Specifically, efforts made in the direction of realizing a unitized regeneration fuel cell (URFC) systems will be outlined and discussed in detail.

Effect of rare earth oxide doping on microstructure and piezoelectric properties of BCTSZ ceramics

Effect of rare earth oxide doping on microstructure and piezoelectric properties of BCTSZ ceramics

Comprehensive study for radiation shielding features for Bi2O3–B2O3–ZnO composite using computational radioanalytical Phy-X/PSD, MCNP5, and SRIM software

The current study uses zinc oxide doping nanoparticles to investigate the radiation shielding properties of bismuth borate glass. Fourier transform infrared (FTIR) and X-ray diffraction (XRD) examined the structural characteristics of the current samples. In contrast, the optical properties were determined based on the absorption spectrum for current samples. Appraisal studies are carried out depending on the simulation capabilities of Phy-X/PSD software in conjunction with MCNP5 to achieve this goal. In addition, the neutron and charged particle shielding properties were evaluated theoretically. All glasses are amorphous, as confirmed by the XRD data, and the FTIR data showed several vibration bands and functional groups. The density showed rising from 5.981 to 6.433 g/cm3 with adding ZnO. The band gap values reduced from 2.831 to 2.091 eV for direct and 3.024 to 2.218 eV for indirect with adding ZnO. The investigations' findings demonstrate a strong agreement between the theoretical and simulation-derived estimates of the mass attenuation coefficient. The relative difference of MAC results lie in the range 0.106–2.941% for BBZ0, 0.105–4.348% for BBZ1, 0.105–3.398% for BBZ2, and 0.105–2.032% for BBZ3. The study's findings are valuable insights from thoroughly examining these parameters, which can potentially improve the radiation protection abilities of Bi2O3–B2O3–ZnO glasses. This study represents a significant step in developing more efficient and safer materials for gamma radiation shielding applications.

Effect of Manganese Oxide Doping of Tin Oxide Thin Films on the Optical and Structural Properties

Tin oxide pure and manganese oxide doped (SnO2:Mn2O3) films were grown on a glass substrate in vacuum by pulsed laser deposition (PLD) technique (using Nd: YAG Laser) at different ratios of Mn2O3 (0, 3, 5, 7, 9) % wt. The structural and optical properties were studied. The X-ray diffraction (XRD) studies showed the structure nature of the films to be polycrystalline and rutile tetragonal. The optical transmittance spectra and optical constants of the prepared thin films, such as extinction coefficient (k), refractive index (n), and real (εr) and imaginary parts (εi) of the dielectric constant, were investigated. The values of the energy band gap increased from 3.5 eV to 3.55 eV with increasing the doping concentration.

Trends in the oxygen adsorption energy derived from the thermodynamic potential model for the oxygen evolution reaction

Across the last years, substantial efforts were done to understand the limitations of the oxygen evolution reaction (OER) catalysts and to develop robust ones such as to solve the efficiency problem in water splitting. Fundamental understanding represents a pathway towards designing superior catalysts. In this direction, several descriptors (ηTD, ESSI, Gmax(η)) have been derived based on the adsorption energies of the OER intermediate moieties (∆EHO*/∆EO*/∆EHOO*) for faster screening of the materials. A universal scaling between the adsorption energies of HO* and HOO* was established for a wide range of materials and in many cases was shown to govern the minimum theoretical overpotential. On the other hand, the scaling between the adsorption energies of HO* and O* fragments have a large scattering along the trendline. In this work we derive five trends for the O* adsorption energies based on theoretical overpotential intervals, using data collected from the published studies employing DFT calculations for OER. It is shown that the best materials have an adsorption energy for HO* placed within a limited interval, yet sufficiently large for a pool of promising catalysts (-0.5,1.5 eV), and that the adsorption energies of O* scales with that of HO* at a slope of one and an intercept of 1.81 eV. Furthermore, a decrease of the intercept for the scaling between HOO* and HO* from 3.14 (valid for all data analyzed) to 3.03 eV is found. For three of the other four trends, the slope of the adsorption energies of O*/HO*scaling is one with intercepts closer either to HOO* (2.2/2.78) or to HO*(1.43/0.78) adsorption energies. For each set of data, the scaling between HOO* and HO* adsorption energies varies from 3 to 3.37 eV. Separately, the trends for O* adsorption energies were analyzed for the TiO2(110) semiconducting rutile surface when doped with transition metals and modified (i) with HO* or H* co-adsorbed fragments that act as charge donor/acceptor moieties or (ii) when the surface was provided with an excess or a lack of electrons. The analysis was performed using the data collected from the published literature, supplemented by additional calculations. Clear trends based on the amount of charge were obtained when standard GGA functionals were used. An understanding for the origin of the large variation of the oxygen adsorption energies for the systems that have similar adsorption energies for the HO*/HOO* is provided. However, when the Hubbard corrected GGA functional is used, some trends change. Clearly, it is still a challenge describing accurately and in a cost-effective manner the adsorption of OER moieties on the undoped or doped transition metal oxides, especially for O*. A strategy to get further insight into the origin of large variations of oxygen adsorption energies for the materials that have similar adsorption energies of HO* and HOO* is discussed.

Investigating the synergetic effect of tungsten oxide doping into the 1,3-dicarbonyl moiety grafted chitosan and phytic acid impregnated sodium alginate for efficient U(VI) adsorption

In this work, chemical modification of the chitosan with ethyl acetoacetate was performed through a base-catalyzed reaction in which epichlorohydrin facilitated the insertion as well as nucleophilic substitution reaction to graft the 1,3-dioxo moiety across the linear chains of the base biopolymer to establish specificity and selectivity for U(VI) removal. The modified chitosan (EAA-CS) was intercalated into phosphate rich alginate matrix (PASA). Later on, the WO3-doped composites with different WO3 to PASA mass ratio were prepared and characterized using FTIR, XPS, SEM-EDS, XRD, and elemental mapping analysis. WO3 significantly contributed to chemically stable inorganic-organic composites with improved porous texture. Among the prepared composites, MCPS-3 microspherical beads, having mass ratio of 30.0 % w/w, exhibited excellent sorption capacity for U(VI) at an optimal pH 4.5. The successful U(VI) sorption was validated by the existence of two U4f peaks at 392.25 and 381.36 eV due to U4f5/2 and U4f7/2 sub-peaks with an intensity ratio of 3:4, respectively. Batch mode sorption kinetics followed pseudo-second-order rate equation (R2 ≈ 0.99, qe,th ≈ 116.88 mg/g, k2 = 0.86 × 10−4 g/mg.min−1) and equilibrium sorption data aligns with Langmuir (R2 = 0.99, qm = 343.85 mg/g at 310 K and pH = 4.5, KL = 2.00 × 10−2 L/mg) and Temkin models (R2 ≈ 0.99). Thermodynamic parameters ΔHo (30.51 kJ/mol), ΔSo (0.19 kJ/mol.K) and ΔGo (−25.64, −26.89, and − 27.91 kJ/mol) at 298, 305, and 310 K, respectively, suggested that the uptake process is feasible, endothermic and spontaneous. Based on these findings, it is reasonable to conclude that MCPS-3 could be a better hydrogel-based biomaterial for appreciable uranium recovery.

The electrical properties and in vitro osteogenic properties of 3D‐printed MgO@BT/HA piezoelectric ceramic disk

AbstractThe repair of bone defects from various causes remains a significant challenge in clinical settings. Piezoelectric materials have been demonstrated to promote osteogenic differentiation, among which barium titanate (BT) has been widely reported. Magnesium oxide (MgO) dopants not only enhance the piezoelectric properties but also stimulate the osteogenic and angiogenic properties in stem cells. In this study, a MgO‐modified BT/hydroxyapatite (MgO@BT/HA) piezoelectric ceramic scaffold was constructed using three‐dimensional (3D)‐printed technology. The results indicated that the addition of MgO improved the electrical properties of BT (d33 = 68.26 pC/N), and facilitated an increase in the proportion of HA (30%) while maintaining the piezoelectric coefficient (d33 = 2.04 pC/N) of the ceramic system. Furthermore, under the induction of low‐intensity pulsed ultrasound (LIPUS) stimulation, in vitro biosafety experiments confirmed that MgO@BT/HA exhibits excellent biosafety and promotes the osteogenic differentiation of dental pulp stem cells (DPSCs).

Surfactant assisted wet chemical synthesis of Cu doped NiO@CNF nanocomposites and their photocatalytic behaviour in degrading brilliant green dye under UV light irradiation

This manuscript details the synthesis of pure NiO and various concentrations of Cu-doped NiO using a simple co-precipitation method, with particular amount of carbon nanoflake (CNF) loading. The prepared materials were initially characterized using X-ray diffraction, scanning electron microscopy with EDAX, transmission electron microscopy, energy dispersive X-ray. Further, UV-diffusion reflectance spectra studies were conducted to explore the optical properties of the prepared nanocomposites. XPS was utilized to explore the surface chemical states and interactions. The XRD pattern analysis revealed that both pure NiO and Cu-doped NiO nanoparticles (NPs) exhibited a face-centered cubic structure. Subsequently, the photocatalytic efficiency of the synthesized samples was evaluated for the degradation of the organic pollutant like brilliant green (BG) under UV light irradiation. Significantly, 30 mol % Cu-doped NiO@CNF nanocomposite demonstrated an enhanced photocatalytic efficiency (97 %) in degrading BG dye when compared to doped oxide materials under UV light. Moreover, the stability of the catalyst was outstanding, and it was effectively reused for five consecutive cycles.

Development of High Performance Thermoelectric Polymers via Doping or Dedoping Engineering.

It is of great significance to develop high-performance thermoelectric (TE) materials, because they can be used to harvest waste heat into electricity and there is abundant waste heat on earth. The conventional TE materials are inorganic semimetals or semiconductors like Bi2Te3 and its derivatives. However, they have problems of high cost, scarce/toxic elements, high thermal conductivity, and poor mechanical flexibility. Organic TE materials emerged as the next-generation TE materials because of their merits including solution processability, low cost, abundant element, low intrinsic thermal conductivity, and high mechanical flexibility. Organic TE materials are mainly conducting polymers because of their high conductivity. Both the conductivity and Seebeck coefficient depend on the doping level, and they are interdependent. Hence, the TE properties of polymers can be improved through doping/dedoping engineering. There are three types of doping forms, oxidative (or reductive) doping, protonic acid doping, and charge transfer doping. Accordingly, they can be dedoped by different approaches. In this article, we review the methods to dope and dedope p-type and n-type TE polymers and the combination of doping and dedoping to optimize their TE properties. Secondary doping is also covered, since it can significantly enhance the conductivity of some TE polymers.

Enhanced sintering resistance in LaYbZr2O7 system through HfO2 doping for thermal insulation ceramic materials

AbstractThe increase in operating temperature contributes to improving the performance and fuel utilization efficiency of gas turbines. However, it also places thermal barrier coatings (TBCs) in a more demanding working environment, requiring higher sintering resistance and better mechanical properties. In the present study, HfO2 was introduced into the dual‐phase LaYbZr2O7 system as a doping oxide to form the LaYb(HfxZr1−x)2O7 system. The research concentrated on its phase composition, mechanical properties, and thermophysical properties. The results show that substituting Hf for Zr does not alter the dual‐phase structure of the system. The mutual inhibition between the two phases and the inherent material‐binding capability of Hf further reduce the grain size compared to pure LYZO. Additionally, the presence of Hf reduces the tendency of Frenkel defect formation and cation migration frequency, effectively inhibiting ion diffusion and thereby suppressing the densification and shrinkage trends of the material. The system retains relatively high hardness, fracture toughness, and low elastic modulus of the LYZO matrix, with a decrease in thermal conductivity and an increase in infrared reflectivity. These results suggest that Hf doping enhances the sintering resistance of LYZO material, making them promising for high‐temperature TBCs. Our study presents a viable approach to enhance the sintering resistance of LYZO, and this methodology can be extrapolated to other rare‐earth zirconates.

Effect of La2O3 on the optical, thermal, structural and radiation shielding properties of TeO2–ZnO–BaO glasses

Influence of lanthanum oxide (La2O3) on various properties of melt quenched zinc barium tellurite glasses (TeO2–BaO–ZnO) have been investigated. Lanthanum was limited to 10 mol% beyond which the glass formation ability was affected leading to crystallization in the proposed tie-line. Glass transition temperature improved with lanthanum oxide incorporation, while the density and energy band gap values showed a minimum at 5 mol%. The observed variation with lanthanum oxide doping was clearly elucidated from Raman spectral data, which indicated their influence in modifying the host ternary glass network. Radiation shielding parameter calculations showed a larger mass and linear attenuation coefficients for glasses doped with 10 mol% lanthanum oxide, indicating the influence of heavier oxides in improving the shielding properties and consequently acting as replacement candidate for toxic lead-based compounds.

Ti4+ doped high-entropy fluorite oxide ceramics ((ZrHfCeYEr)(1-x)/5Tix)O2-δ: Thermal, mechanical and cyclic thermal shock resistance properties studies

High-entropy fluorite oxide ceramics are promising candidates for spacecraft applications due to their excellent high-temperature thermal-mechanical properties. In this work, four kinds of high-entropy fluorite oxide ceramics ((ZrHfCeYEr)(1-x)/5Tix)O2-δ (HEFOs, x = 0, 0.025, 0.05, 0.075) with different Ti4+ contents were successfully synthesized through solid-state reaction method with conventional sintering. They all exhibited phase stability when annealed at 1500 ℃ for 20 h. When the content of Ti4+ was increased to x = 0.075, the thermal conductivity reduced to1.34 W·m−1·K−1 at 1100 ℃, and the hardness and elastic modulus increased to 14.01 GPa and 205.70 GPa, respectively. Furthermore, the cyclic thermal shock resistance of HEFOs at different temperatures was investigated. The initial flexural strength reached 219.03 MPa when the content of Ti4+ was increased to x = 0.075. After 60 thermal shock cycles at 1200 ℃ and 1500 ℃, the residual strength ratios were 97.56 % and 83.36 %, respectively. The results of this study establish the foundation for future applications of high-entropy fluorite oxide ceramics in spacecraft hot-end components.

Over 19% Efficient Inverted Organic Photovoltaics Featuring a Molecularly Doped Metal Oxide Electron-Transporting Layer.

Molecular doping is commonly utilized to tune the charge transport properties of organic semiconductors. However, applying this technique to electrically dope inorganic materials like metal oxide semiconductors is challenging due to the limited availability of molecules with suitable energy levels and processing characteristics. Herein, n-type doping of zinc oxide (ZnO) films is demonstrated using 1,3-dimethylimidazolium-2-carboxylate (CO2-DMI), a thermally activated organic n-type dopant. Adding CO2-DMI into the ZnO precursor solution and processing it atop a predeposited indium oxide (InOx) layer yield InOx/n-ZnO heterojunctions with increased electron field-effect mobility of 32.6 cm2 V-1 s-1 compared to 18.5 cm2 V-1 s-1 for the pristine InOx/ZnO bilayer. The improved electron transport originates from the ZnO's enhanced crystallinity, reduced hydroxyl concentrations, and fewer oxygen vacancy groups upon doping. Applying the optimally doped InOx/n-ZnO heterojunctions as the electron-transporting layers (ETLs) in organic photovoltaics (OPVs) yields cells with improved power conversion efficiency of 19.06%, up from 18.3% for devices with pristine ZnO, and 18.2% for devices featuring the undoped InOx/ZnO ETL. It is shown that the all-around improved OPV performance originates from synergistic effects associated with CO2-DMI doping of the thermally grown ZnO, highlighting its potential as an electronic dopant for ZnO and potentially other metal oxides.

Pt single-atom electrocatalysts at Cu2O nanowires for boosting electrochemical sensing toward glucose

In electrochemical biosensors, rational design and synthesis of high-performance electrochemical glucose sensors based on emerging single-atom catalysts (SACs) are paramount. Herein, a facile approach is proposed for dispersing single-atom doping of cuprous oxide (Cu2O) nanowires with Pt on a copper foam substrate (Pt1/Cu2O@CF) via the electrochemical deposition process. The specific nanostructure of the single-atom catalyst has been elaborately revealed with the aid of atomic resolution scanning transmission electron microscopy (STEM) and X-ray absorption fine structure spectroscopy (XAS). The as-fabricated Pt1/Cu2O@CF biosensor with satisfactory scalability exhibits a low limit of detection (1 μM), ultrahigh sensitivity (31.55 mA mM−1 cm−2), excellent selectivity, and robust reliability toward glucose. The first principles simulations reveal that Pt SAC is beneficial to the adsorption of glucose on the surface and further facilitates the electron transfer for the deprotonation process, resulting in high glucose sensing performance. This work sheds light on the applications of SACs for designing ultrasensitive electrochemical biosensors.

Adsorption of dissolved gases (CO, H2, CO2) produced by partial discharge in converter transformer oil by CuO(1, 2) and Ag2O(1, 2) clusters doped with MoTe2: A DFT study

Density functional theory (DFT) was used to analyze the effect of (CuO)n, (Ag2O)n (n=1, 2) cluster-doped MoTe2 on the three gases (CO, H2 and CO2) adsorption performance and characteristics. MoTe2 has large bond length and low binding energy, which can simultaneously achieve high sensitivity to target molecules and excellent reversibility at room temperature. By analyzing the modified MoTe2, compared with the initial MoTe2, the reduced energy band structure of band gap, the increased adsorption energy, more charge transfer, and the increased conductivity of DOS, all reflect that the doping of metal oxides enhances the adsorption and sensing performance of MoTe2 for the three gases. The adsorption capacity of CuO-MoTe2 and (Ag2O)2-MoTe2 for the three gases is: CO>H2>CO2, while the adsorption capacity of (CuO)2-MoTe2 and Ag2O-MoTe2 for the three gases is: CO>CO2>H2. Finally, the adsorption effects of the four modifications were compared and feasibility analyzed through molecular orbitals, recovery time, sensitivity and work function, and corresponding conclusions were drawn. The results of this study provide a theoretical basis for detecting dissolved gases in oil generated by partial discharge of converter transformers.

Rb-Doped Perovskite Oxides: Surface Enrichment and Structural Reconstruction During the Oxygen Evolution Reaction.

Alkali-metal doped perovskite oxides have emerged as promising materials due to their unique properties and broad applications in various fields, including photovoltaics and catalysis. Understanding the complex interplay between alkali metal doping, structural modifications, and their impact on performance remains a crucial challenge. In this study, this challenge is addressed by investigating the synthesis and properties of Rb-doped perovskite oxides. These results reveal that the doping of Rb into perovskite oxides function as a structural modifier in the as-synthesized samples and during the oxygen evolution reaction (OER) as well. Electron microscopy and first-principles calculations confirm the enrichment of Rb on the surface of the as-synthesized sample. Further investigations into the electrocatalytic reaction revealed that the Rb-doped perovskite underwent drastic restructuring with Rb leaching and formation of strontium oxide.

How Depletion Layers Govern the Dynamic Plasmonic Response of In-Doped CdO Nanocrystals.

Doped metal oxide nanocrystals exhibit a localized surface plasmon resonance that is widely tunable across the mid- to near-infrared region, making them useful for applications in optoelectronics, sensing, and photocatalysis. Surface states pin the Fermi level and induce a surface depletion layer that hinders conductivity and refractive index sensing but can be advantageous for optical modulation. Several strategies have been developed to both synthetically and postsynthetically tailor the depletion layer toward particular applications; however, this understanding has primarily been advanced in Sn-doped In2O3 (ITO) nanocrystals, leaving open questions about generalizing to other doped metal oxides. Here, we quantitatively analyze the depletion layer in In-doped CdO (ICO) nanocrystals, which is shown to have an intrinsically wide depletion layer that leads to broad plasmonic modulation via postsynthetic chemical reduction and ligand exchange. Leveraging these insights, we applied depletion layer tuning to enhance the inherently weak plasmonic coupling in ICO nanocrystal superlattices. Our results demonstrate how an electronic band structure dictates the radial distribution of electrons and governs the response to postsynthetic modulation, enabling the design of tunable and responsive plasmonic materials.